USA-based Genitope Corp has suspended development of MyVax, its investigational personalized immunotherapy, and is evaluating its alternatives with respect to the other aspects of its business, including development of its monoclonal antibody program.
The firm made the announcement after a meeting with representatives of the US Food and Drug Administration to discuss the previously-announced results of a pivotal Phase III clinical trial of MyVax personalized immunotherapy in previously-untreated follicular B-cell non-Hodgkin's lymphoma patients. The study did not meet its primary endpoint - there was no statistically-significant difference in progression-free survival with the agent versus the control.
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